Product Safety Recalls

Product Recall Tracker

Siemens Medical Solutions USA, Inc Recall 87479

Description: Interventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.

Siemens Medical Solutions USA, Inc Recall 87479 Information

StatusTerminated
Mandated?Voluntary: Firm initiated
Recall NumberZ-1288-2021
Event ID87479
Event DescriptionInterventional Fluoroscopic X-Ray System - Product Usage: developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
Product TypeDevices
DistributionUS Nationwide distribution in the states of MI, KY, TX.
Quantity29 systems
Recall ReasonSiemens has become aware of a potential issue in which the imaging system UPS sporadically forces a shutdown of the imaging system PC without a true power supply problem.
Device Classification20210331
Device Code InfoARTIS Icono biplane- 11327600 ARTIS Icono floor- 11327700
Center Classification Date20210322
Recall Initiation Date20210226
Recalling FirmSiemens Medical Solutions USA, Inc
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.